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FDA 510(k)

CAPD U.V. GERMICIDAL CONNECTION SYSTEM

K-Number: K812802 · 1982-03-02

Decision Date1982-03-02
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAPD U.V. GERMICIDAL CONNECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1982-03-02 under 510(k) number K812802. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPD U.V. GERMICIDAL CONNECTION SYSTEM?

CAPD U.V. GERMICIDAL CONNECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K812802.

When did CAPD U.V. GERMICIDAL CONNECTION SYSTEM receive FDA 510(k) clearance?

CAPD U.V. GERMICIDAL CONNECTION SYSTEM received FDA 510(k) clearance on 1982-03-02, under 510(k) number K812802.

Who is the listed applicant for CAPD U.V. GERMICIDAL CONNECTION SYSTEM?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPD U.V. GERMICIDAL CONNECTION SYSTEM?

The FDA product code for CAPD U.V. GERMICIDAL CONNECTION SYSTEM is KDJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Travenol Laboratories, S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 206 devices →

Related Devices (Code: KDJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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